57987-55-0

Usage

Uses

Used in Chemical Industry:
2,4-DIETHYL-1,5-PENTANEDIOL is used as a solvent for various chemical reactions, providing a medium that facilitates the process and improves the efficiency of the reaction.
Used in Plastics Industry:
As a plasticizer, 2,4-DIETHYL-1,5-PENTANEDIOL is utilized to increase the flexibility and workability of plastic materials, enhancing their performance in various applications.
Used in Personal Care Products:
2,4-DIETHYL-1,5-PENTANEDIOL is used as an ingredient in some personal care products, contributing to their formulation and potentially offering benefits such as improved texture and consistency.
Used in Pharmaceutical Formulations:
In the pharmaceutical industry, 2,4-DIETHYL-1,5-PENTANEDIOL may be employed as a component in drug formulations, potentially aiding in the delivery and effectiveness of medications.
Used in Polymer Synthesis:
2,4-DIETHYL-1,5-PENTANEDIOL has potential applications as a monomer in the synthesis of polymers, which can be used in a wide range of products, from plastics to textiles.
Used in Specialty Chemicals Production:
As a component in the production of specialty chemicals, 2,4-DIETHYL-1,5-PENTANEDIOL contributes to the creation of unique chemical products with specific properties for targeted applications.

InChI:InChI=1/C9H20O2/c1-3-8(6-10)5-9(4-2)7-11/h8-11H,3-7H2,1-2H3

Upstream product

• 27899-21-4 2,4-diethylglutaric acid 
• 50-00-0 formaldehyd 
• 64344-45-2 (E)-2-ethyl-2-hexenal 

Downstream Products

• 27899-21-4 2,4-diethylglutaric acid 

Relevant academic research and scientific papers

Iron(II) pincer-catalyzed synthesis of lactones and lactams through a versatile dehydrogenative domino sequence

The synthesis of lactones and lactams by using iron(II) pincer-catalyzed dehydrogenative methodology was developed. Starting from 1,n-diols or 1,n-amino alcohols, this domino transformation takes place through initial dehydrogenation of the substrates, subsequent intramolecular cyclization, and final oxidation to afford the desired products in good yields. The ability to access heterocycles of different sizes makes this protocol especially versatile, in which two consecutive oxidation reactions are performed without requiring an external oxidant. In this paper, we report the application of the Fe-MACHO-BH complex [carbonylhydrido(tetrahydroborato)[bis(2-diisopropylphosphinoethyl)amino]iron(II)] in this atom-efficient and environmentally benign process, for which molecular hydrogen is formed as the only stoichiometric side product. Just a little pinch: The iron(II) pincer-catalyzed synthesis of lactones and lactams from easily available 1,n-diols and 1,n-amino alcohols is explored. The use of a nontoxic metal as well as the generation of molecular hydrogen as the only stoichiometric byproduct makes this method a highly atom-efficient and environmentally benign process.

Process for producing 1,5-pentanediol derivatives

(In the formulae, R1 and R2, which may be the same or different, each represents hydrogen or lower alkyl.) The present invention relates to a process for producing 1,5-pentanediol derivatives represented by general formula (II) which comprises reacting 2-butenal derivatives represented by general formula (I) with formaldehyde, and hydrogenating the obtained mixture of reaction products.